Halogenated cyclopropyl and cyclopropenyl estratrienes and process for their preparation



United States Patent 3,385,871 HALOGENATED CYCLOPRQPYL AND CYCLQ- PROPENYL ESTRATRIENES AND PRDCESS FGR THEIR EREPARATHQN John A. Edwards, Palo Alto, Calif., and Lawrence H.

Knox, Mexico City, Mexico, assignors to Syntax Corporation, Panama, Panama, a corporation of Panama No Drawing. Filed Dec. 15, 1965, Ser. No. 514,136 17 (Ilaims. (Ci. 26tl397.4)

ABSTRACT OF THE DISCLQSURE Steroids having an aromatic A-ring and substituted at C17 with a dihalocyclopropyl, dihalocyclopropenyl, or oxocyclopropenyl group useful as estrogenic agents.

This invention relates to novel steroids and to processes for their preparation. Specifically, this invention is directed at steroids of the formula:

wherein The hydrocarbon carboxylic acyl and acyloxy groups of the present invention contain less than 12 carbon atoms and may be of a straight, branched, cyclic or cyclicaliphatic chain structure. This structure may be saturated, unsaturated, or aromatic and optionally substituted by functional groups such as hydroxy, alkoxy containing up to 5 carbon atoms, acyloxy containing up to 12 carbon atoms, nitro, amino, halogeno, and the like..Typical esters thus include acetate, propionate, enanthate, benzoate, trimethylacetate, t-butylacetate, phenoxyacetate, cyclopentylpropionate, aminoacetate, ,B-chloropropionate, adamantoate, and the like.

The novel steroids provided by this invention demonstrate estrogenic activity and are useful in the treatment of the various conditions in which such agents are indicated, such as estrogen deficiencies, menopause, and the like. These compounds may also be used in veterinary medicine in the same manner as known estrogens and in the control and regulation of fertility. In addition, these agents demonstrate antiandrogen activity. They may be administered in the usual pharmaceutical forms at dosages appropriate for the condition being treated.

These compounds are prepared according to a process which may be represented as follows:

. .C-C-R ice wherein R R R R Z, X and Y are as previously defined, and Z is a carbon-carbon double bond or a carbon-carbon triple bond.

In the practice of the foregoing transformation, an estra-l,3,5(10)-triene having vinyl, l-propenyl, chlorovinyl, ethynyl, l-propynyl or chloroethynyl group in the L-pOSltiOH (I) is treated with a dihalocarbene, as is generated for example from alkali metal salts of trihaloacetic acid, e.g., sodium trichloroacetate, sodium chlorodifiuoroacetate, and sodium dichlorofluoroacetate, to yield the corresponding 17a-dihalocyclopropyl (Z single bond) or l7e-dihalocyclopropenyl (Z=d0uble bond) derivatives of Formula II. The reaction is executed under anhydrous conditions in an inert organic solvent such as diethylene glycol dimethyl ether, triethylene glycol di methyl ether, or the like. The product forms directly and may be readily separated from the reaction mixture by conventional methods. Likewise, other reagents known to generate dihalocarbenes, such as trimethyl (trifluoromethyl) tin, phenyl (trichloromethyl) mercury, phenyl (bromodichloromethyl) mercury and the like, with sodium iodide, may also be used in a similar fashion.

The requisite starting material of Formula I wherein Z is a triple bond is readily prepared from the corresponding l7-keto compound through conventional methods, e.g., treatment with acetylene and potassium t-butoxide, use of dichloroethylene and methyl lithium, use of alkynyl magnesium halides, and the like. The starting materials wherein Z is a double bond are preferably obtained from the corresponding Uni-alkynyl compounds through controlled hydrogenation according to conventional procedures.

The resulting -hydroxy-17a-alkeny1 or -17 x-alkyny1 compounds may be converted to the corresponding 17,3- acyloxy or 17 B-tetrahydropyranyloxy derivatives via conventional methods prior to practicing the process of this invention or may be subjected thereto directly and, if desired, etherified or esterified thereafter.

The substituent in the 3-position of the estratriene nucleus of the compounds of the present invention may be a hydroxy group or an etherified, e.g., methoxy, tetrahydropyranyloxy etc., or esterified, e.g., acetoxy, benzoyloxy, etc., derivative thereof. These derivatives may be formed prior to the principal reaction of the present invention or may be formed thereafter via conventional methods. Thus, treatment with an appropriate acid anhydride, such as acetic anhydride, in pyridine with a 3,175- dihydroxy compound of the present invention yields the 3- acyloxy-17B-hydroxy derivative selectively. Use of an acid anhydride in the presence of the corresponding acid and an acid catalyst such as p-toluenesulfonic acid yield the 3,17fi-diacyloxy derivative. This diester may then be selectively saponified as through the use of methanolic potassium bicarbonate to yield the corresponding 3-hydroxy- 17,8-acyloxy derivative. Similarly, etherification may be performed via conventional procedures. Thus, treatment with dihydropyran in the presence of an acid catalyst such as p-toluenesulfonic acid, p-toluenesulfonyl chloride, dinitrobenzene sulfonic acid or the like, yield the corresponding tetrahydropyranyloxy derivative. Formation of the monotetrahydropyranyl ether may be accomplished by selective protection of other hydroxy groups as through alents of sodium trichloroacetate in 40 ml. of diethylene ester formation, in the manner described above, with glycol dimethyl ether. After refluxing for an additional alkaline hydrolysis of such ester groups after formation hour, the mixture is filtered. The filtrate is evaporated to of the tetrahydropyranyl ether. Formation of S-methoxy dryness and the residue is chromatographed on alumina, derivatives may likewise be realized through the use of 5 cluting with methylene chloride, to yield 3-methoxy-l7adimethylsulfate and potassium hydroxide. (2',2-dichlorocyclopropyl) 17fl-acetoxyestra-l,3,5(10)- The 17a-dihalocyclopropenyl derivatives of the present triene. invention may be catalytically hydrogenated as with 5% In a like fashion, 3-methoxy-l7a-vinyl-l7fi-acetoxyd8 palladium-on-charcoal to yield the corresponding dihalomethylestra-l,3,5()-triene and 17a-vinyl l7fi-acetoxycyclopropyl derivatives. 10 estra-l,3,5(10)-trien-3-ol are subjected to the foregomg In addition to the biological properties described above, procedure to yield S-methoxy-17a-(2,2-dichlorocycloprothe compounds of the present invention also serve as inpyl) 17B-acetoxy l8-methylestra 1,3,5 l0)-triene and termediates for the preparation of other novel estrogenic 171x (2',2-dichlorocyclopropyl) 17/3-acetoxyestra-L3, agents. Thus, treatment of a 17a-dihalocyclopropyl com- 5(10)-trien-3-ol, respectively. pound of the present invention with magnesium or an By use of sodium chlorodifluoroacetate in the foregoalkyl lithium reagent yields the corresponding 17a-propaing procedure, there is obtained, respectively, 3-methoxydienyl derivative. This transformation may be represented 17:: (2,2-difluorocyclopropyl) l7/3-acetoxyestra 1,3, as follows: 5 (10)-triene; 3-methoxy 17a-(2,2'-difluorocyclopropyl)- In the foregoing transformation, R R and R are as 17B-acetoxy IS-methylestra 1,3,5(l0)-triene and 1711- described above. R is preferably hydroxy, methoxy or (2',2'-difiuorocyclopropyl) -17fl-acetoxyestra-1,3,5(10)- acyloxy with the corresponding 3-tetrahydropyranyloxy 3 trien-3-ol. derivatives being thereafter obtained from the correspond- The corresponding 17B-hydroxy derivatives may be ing -3-hydroxy compound via the procedure described alternatively used in the foregoing procedure, the prodabove. This ring opening dehalogenation is preferably ucts thus obtained being similarly unesterified in the 17/3- performed with those compounds wherein X and Y are position, i.e. 3-methoxy 17a-(2',2-dichlorocyclopropyl)- chloro. In addition, compounds having a structure identiestra 1,3,5 (l0)-trien 17/3-ol, S-methoxy 17oc-(2',2'-dical to that shown in Formula 111 but characterized by chlorocyclopropyl) -18-methylestra -1,3,5(10)-trien-17B- both X and Y being bromo groups are particularly useful 01, 1704 (2',2'-dichlorocyclopropyl)-estra 1,3,5(l0)-triintermediates for the preparation of l7a-propadienyl deene-3,17,B-diol, 3-methoxy 17a(2',2'-difiuorocycloproprivatives of Formula IV. Such l7a-dibromocyclopropyl 4O yl)-estra 1,3,5-trien 175-01, 3-methoxy 17ot-(2,2'-dicompounds are readily prepared through the action of fluorocyclopropyl) IS-methylestra- 1,3,5(10)-trien-l7fibromoform and potassium t-butoxide on a l7a-vinyl de- 01, and 17a(2',2-difluorocyclopropyl)-estra 1,3,5-( 10)- rivative of Formula I. The resultant 17u-dibromocyclotriene-3,l7,8-diol. propyl compound is then subjected to the action of mag- The requisite 3 methoxy 170: vinyl-l7fl-acetoxy-18- nesium, as described above for the corresponding 17a-dimethylestra-l,3,5(lO)-triene starting material may be obchlorocyclopropyl derivative. U tained in the following manner.

Brief acid hydrolysis, as with formic acid or hydro- A solution of 1 g. of 3-methoxy-18-methylestra-l,3,

chloric acid, of the 17a-dihalocyclopropenyl compounds 5(l0)-trien-17-one in ml. of anhydrous benzene is (Z=double bond) of the present invention results in added under nitrogen to a solution of 1.4 g. of potassium formation of the corresponding 17a-cyclopropenones. This in 30 ml. of t-amyl alcohol. A slow current of purified transformation may be represented as follows: 5 acetylene is then passed through the solution for hours.

. (B C-R in which R R R R and X and Y are as previously The mixture is diluted with water and extracted with bendefined. zene. These extracts are washed with water to neutrality, As heremabove described, compounds of Formulas IV dried over sodium sulfate and evaporated. Chromatogand VI are estrogemc agents which may be used in the raphy of the residue on alkaline alumina with 2:3 hexane:

same fashion as the l7a-halocyclopropyl and 17a-halobenzene yields 3 -methoxy-17a-ethynyl-18-methylestra-l,

cyclopropenyl compounds of the present mvention. 3,5(l0)-trien-17,B-ol which is recrystallized from acetone:

The following examples will serve to typify the nature hexane.

of this invention but, being presented only for purposes A solution of l g. of 3-methoxy-l7u-ethynyl-lS-methylof illustration, they should not be construed as a limitaestra-l 3 5 10 -t tion thereof. I men 17 8 01 m 40 ml. of pyrldme is by EXAMPLE 1 presence of 0.4 g. of prehydrogenated 2% palladium-on- To a efl xi g solution of 1 g, of 3 h 7 calcium carbonate until 1.1 molar equivalents of hydro- 17p-acetoxyestra-1,3,5(10)-triene in 10 ml. of diethylene g are absorbed- The Catalyst is removed y filtration glycol dirnet-hyl ether is added over a two hour period through Celite diatomaceous earth and washed with ethyl in a dropwise fashion with stirring, a solution of 35 equiv- 75 acetate and the combined filtrate and washings are evapodrogenated at 25 C. and atmospheric pressure in the rated to dryness under reduced pressure. The residue is dissolved in ethyl acetate and this solution is then washed with dilute hydrochloric acid and water to neutrality, dried and evaporated to dryness to yield 3-methoxy-17uvinyl-18-methylestra-1,3,5(l0)-trien-17fi-ol which is further purified through recrystallization from acetone.

A mixture of 1 g. of 3-methoxy-17a-vinyl-l8-methylestra-1,3,5(10)-trien-17{i-ol, 1 g. of p-toluenesulfonic acid monohydrate, 50 ml. of acetic acid and 25 ml. of acetic anhydride is allowed to stand at room temperature for 24 hours, and then poured into water and stirred. This mixture is then extracted with methylene chloride and these extracts are dried and evaporated to yield 3-methoxy-17ocviny l 17B-acetoxy-18-methylestra-1,3,5(10)-trien which is recrystallized from acetonezether.

3 methoxyl7a-ethynyl-17,8-acetoxy-1S-methylestra- 1,3,5 (10)-triene is obtained in a similar fashion from its corresponding 17t2-hydroxy compound.

EXAMPLE 2 To a solution of 5.0 g. of 17a-ethynyl-17,8-acetoxyestra- 1,3,5 (10)-trien-3-ol in 75 n11. of dry diethylene glycol dimethyl ether is added 4.36 g. of sodium chlorodifluoroacetate. The mixture is heated at reflux for 15 minutes, cooled and an additional 4.36 g. of sodium chlorodifluoroacetate are added and refluxing is continued for 15 more minutes. This procedure is repeated until 17.32 g. of salt have been added. The mixture is then filtered and concentrated in vacuo. The residue is then chromatographed on Florisil absorbent, eluting with ether, to yield 17oc-(2',2'-Clifi1101'0- cyclopropenyl) 17B acetoxyestra l,3,5(10) trien-3-ol which is recrystallized from methanol.

In a similar fashion, 17a-(2,2'-difluorocyclopropenyl)- 17d acetoxy 18 methylestra-l,3,5(10)-trien-3-ol; 3- methoxy 17a-(2',2'-difiuorocyclopropenyl)-17,B-acetoxyestra-1,3,5(10)-trien and 3amethoxy-17u-(2',2-difluorocyclopropenyl 17(3 acetoxy 18 methylestra 1,3,5 (10)- triene are obtained from the corresponding starting materials.

Alternatively, the corresponding free 17 B-hydroxy compounds of the three foregoing starting materials may be employed in this procedure to yield 17u-(2,2'-difiuorocyclopropenyl) estra- 1,3,5(l)-triene-3,17[3-diol; 17u-(2', 2' difluorocyclopropenyD-lS-methylestra-l,3,5(10)-trien- 175-01 and, if desired, these may by acylated.

EXAMPLE 3 By subjecting 3 methoxy 17a-chlor0ethynyl-17fl-acetoxyestra-1,3,5(10)-triene to the procedure of Example 2, there is obtained 3 methoxy 17a (2,2'-difluoro-3'- chlorocyclopropenyl 176 acetoxyestra-1,3,5(10)-triene. Likewise, from 17a-(1'propynyl)-l7B-acet0xyestra-l,3,5 (lO)-trien-3-ol there is obtained 17ot-(2,2difluoro-3 methylcyclopropenyl) 175-acetoxyestra-l,3,5 10) -trien- 3-ol.

EXAMPLE 4 By employing sodium trichloroacetate in the procedure of Example 2, there are respectively obtained 17ot-(2,2' dichlorocyclopropenyl) 175 acetoxyestra l,3,5(10) trien-3-ol; 17a (2',2 dichloropropenyl-17B-acetoxy-l8- methylestra 1,3,5 (10)-trien-3-ol; 3-methoxy-l7tt-(2',2'- dichlorocyclopropenyl) 17/3-acetoxye'stra-1,3,5(10) triene and 3 methoxy 17a-(2,2'-dichlorocyclopropenyl)-175- acetoxy 18-rnethylestra-l,3,5(10)-triene.

EXAMPLE Two milliliters of dihydropyran are added to a solution of 1 g. of 3-methoxy-l7a-(2',2'difluorocyclopropyl) estra-1,3,5()trien-17fl-ol in ml. of benzene. About 1 ml. is removed by distillation to remove moisture and 0.4 g. of p-toluenesulfonic acid is added to the cooled solution. This mixture is allowed to stand at room temperature for 4 days, and is then washed with aqueous s0- dium carbonate solution and water, dried and evaporated. The residue is chromatographed on neutral alumina, eluting with hexane, to yield 3-methoxy-17a-(2,2'-difluorocyclopropyl) 17B- tetrahydropyranyloxyestra-1,3,5(l0)- triene which is recrystallized from pentane.

Use of this process with the other 17,8-hydroxy com pounds of the present invention will similarly yield the corresponding l7fl-tetrahydropyranyloxy derivatives.

EXAMPLE 6 A mixture of 1 g. of 17a-(2,2-dichlorocyclopropyl)- estra-1,3,5 (lO)triene-3,l7fl-diol, 4 ml. of pyridine and 2 ml. of acetic anhydride is allowed to stand at room temperature for 15 hours. The mixture is then poured into ice water and the solid which forms is collected by filtration, washed with water and dried to yield 3-acetoxy-17a- (2,2' dichlorocyclopropyl) estra-1,3,5(10)-trien-l7fi- 01 which may be further purified through recrystallization from acetonerhexane.

In a similar manner, the other 3-hydroxy compounds of the present invention may be selectively converted to the corresponding 3-acetoxy derivatives, as for example 35- acetoxy-(2,2'-difiuorocyclopropenyl) estra 1,3,5 10)- trien-17Bol. Through the use of other anhydrides in the foregoing procedures, the corresponding 3-acylates are similarly prepared.

EXAMPLE 7 A mixture of 1 g. of l7tx-(2,2'-difluorocyclopropyl)- estra-1,3,5(10)-triene-3,17 3-diol, 1 g. of p-toluenesulfonic acid monohydrate, 50 ml. of acetic acid and 25 ml. of acetic anhydride is allowed to stand at room temperature for 24 hours, and then poured into water and stirred. This mixture is then extracted with methylene chloride and these extracts are dried and evaporated to yield 3,1718- diacetoxy 17a. (2',2'-difluorocyclopropyl)-estra 1,3,5 (10)-triene, which is recrystallized from acetonezether.

One gram of 3,17,8-diacetoxy-17u-(2',2'-difluorocyclopropyl)-estra-1,3,5(l0)-triene is allowed to stand at room temperature for 15 hours with 1 g. of potassium bicarbonate in 10 ml. of water and ml. of methanol. At the end of this time, the methanol is evaporated under reduced pressure and the residue is extracted with ethyl acetate and water. Evaporation of the ethyl acetate from these extracts yields l75-acetoxy-17ot-(2,2-difluorocyclopropyl)-estra-1,3,5(10)-trien-3-ol which is collected by filtration and recrystallized from acetonezhexane.

Two milliliters of dihyd-ropyran are added to a solution of 1 g. of -acetoxy 17a (2',2'-difiuorocyclopropyl)- estra-1,3,5(10)-trien-3-ol in 15 ml. of benzene. About 1 ml. is removed by distillation to remove moisture and 0.4 g. of p-toluenesulfonic acid is added to the cooled solution. This mixture is allowed to stand at room temperature for 4 days, and is then washed with aqueous sodium carbonate solution and water, dried and evaporated. The residue is chromatographed on neutral alumina, eluting with hexane, to yield 3-tetrahydropyranyloxy 17/3 acetoxy-17ot-(2',2' difluorocyclopropyl) estra 1,3,5(10)- triene which is recrystallized from pentane.

A solution of 0.17 g. of potassium hydroxide in 0.2 ml. of water and 2.5 ml. of methanol is added over 30 mintues to a refluxing solution of 1 g. of 3-tetrahydropyranyloxy-l7fl-acetoxy 17oz (2',2'-difluorocyclopropyl)-estra-1,3,5(10)-triene in 30 ml. of methanol under nitrogen. The solution is refluxed for 2 hours, cooled, neutralized with acetic acid and concentrated under reduced pressure. After the addition of water, the solid which forms is collected by filtration and dried to yield 3-tetrahydropyranyloxy 17a (2,2'-difiuorocyclopropyl)-estra-1,3,5 (10)trien-17/3-0l which is recrystallized from acetonezhexane.

EXAMPLE 8 Two milliliters of dihydropyran are added to a solution of 1 g. of 3-acetoxy 17a (2,2-dichlorocyclopropyl)- 7 estra-1,3,5(10)-trien-17B-ol in 15 ml. of benzene. About 1 ml. is removed by distillation to remove moisture and 0.4 g. of p-toluenesulfonic acid is added to the cooled solution. This mixture is allowed to stand at room temperature for 4 days, and is then washed with aqueous sodium carbonate solution and water, dried and evaporated. The residue is chromatographed on neutral alumina, eluting with hexane, to yield 3-acetoxy-17a-(2,2- dichlorocyclopropyl) 1713 tetrahydropyranyloxyestra- 1,3,5(10)-triene which is recrystallized from pentane.

One gram of 3-acetoxy-17a-(2,2'-dichlorocyclopropyl)- l7fl-tetrahydropyranloxyestra-l,3,5(lO)-triene is allowed to stand at room temperature for 15 hours with 1 g. of potassium bicarbonate in 10 ml. of water and 90 ml. of methanol. At the end of this time, the methanol is evaporated under reduced pressure and the residue is extracted with ethyl acetate and water. Evaporation of the ethyl acetate from these extracts yields 17u-(2,2-dichlorocyclopropyl) 17,8 tetrahydropyranyloxyestra-1,3,5(10)- trien-S-ol, which is collected by filtration and recrystallized from acetonezhexane.

EXAMPLE 9 To a refluxing solution of 1 g. of 3-methoxy-l7a-(2', 2'-dichlorocyclopropyl) 17 8 acetoxyestra 1,3,5 (10)- triene, 1.3 g. of magnesium shavings, and 25 ml. of anhydrous ether are added over a one hour period 5.7 g. of ethyl bromide. When the addition is complete, the reaction mixture is refluxed an additional hour and then cautiously hydrolyzed by a dropwise addition of water, followed by 10% hydrochloric acid. The ether layer is separated, dried and evaporated to give 3-methoxy-l7a-propadienyl- 1 7p3-acetoxyestra-l ,3 ,5 l) -triene.

By likewise subjecting the other 17u-(2,2'-dihalocyclopropyl) derivatives of the present invention to the procedure of this example, the corresponding 17ct-propadi enyl derivatives are obtained.

EXAMPLE To 3.2 ml. of cold (0") concentrated hydrochloric acid is added with stirring, 0.1 g. of 3-methoxy-17a-(2,2'-difiuorocyclopropenyl) 17B acetoxyestra 1,3,5(10)- triene. The mixture is stirred until the steroid is completely dissolved, then stirred for one additional minute, and finally poured into a mixture of aqueous sodium bicarbonate and ethyl acetate. The organic layer is separated and the aqueous phase extracted with ethyl acetate. The combined organic solutions are then washed with water to neutrality, dried over sodium sulfate and evaporated to dryness to yield 3-methoxy 171x oxocyclopropenyl-17B- acetoxyestra-1,3,5(l0)-triene which may be further purified through recrystallization from methanol.

In a similar fashion the following compounds are obtained from the corresponding l7a-(2',2-difluorocyclopropenyl) via the foregoing procedure 3 -methoxy-17a-oxocyclopropenyl-17,9-acetoxy-l 8- methylestra- 1,3,5 l0) -triene;

3-metl1oxy-17a-oxocyclopropenylestra-1,3,5( l0) trien-l7fl-ol;

2-methoxy-17rx-oxocyclopropenyl-18-methylestra- 1,3,5 (10) -trien-17 8-ol;

17a-OXOCYC1OPIOP8I1Y1- 17fl-acetoxyestra-1,3,5( 10 trien-3 -ol;

17n-oxocyclopropenyl-17 3-acetoxy-18-methylestra- 1,3,5 10)-trien-3-ol;

17a-oxocyclopropenylestra-1,3 ,5 (10)-triene-3,17,B-diol and 17ot-oxocyclopropenylestra-18-methylestra-1,3,5 10

triene-3, l7B-diol.

EXAMPLE 11 Two milliliters of dihydropyran are added to a solution of 1 g. of 1701 oxocyclopropenyl 17p acetoxyestra- 1,3,5(10) trien 3 01 in ml. of benzene. About 1 ml. is removed by distillation to remove moisture and. 0.4 g. of p toluenesulfonyl chloride is added to the cooled solution. This mixture is allowed to stand at room temperature for four days, and is then washed with aqueous sodium carbonate solution and water, dried and evaporated. The residue is chromatographed on neutral alumina, eluting with hexane, to yield 3 tetrahydropyranyloxy 17a oxocyclopropenyl 1718 acetoxyestra 1,3,5 (10) triene which is recrystallized from pentane.

What is claimed is:

1. Compounds of the formula:

wherein R is hydrogen, methyl, tetrahydropyranyl or a hydrocarbon carboxylic acyl group of less than 12 carbon atoms;

R is hydrogen or methyl;

R is hydrogen, tetrahydropyranyl or a hydrocarbon carboxylic acyl group of less than 12 carbon atoms;

R is hydrogen, methyl or chloro;

each of X and R is chloro or fiuoro; and

Z is a carbon-carbon single bond or a carbon-carbon double bond.

2. Compounds according to claim 1 wherein Z is a carbon-carbon single bond;

each of X and R is fluoro;

R is hydrogen; and

R R and R are as therein defined.

3. The compound according to claim 2 wherein R is hydrogen;

R is hydrogen; and

R is hydrogen.

4. The compound according to claim 2 wherein R is methyl;

R is hydrogen; and

R is hydrogen.

5. The compound according to claim 2 wherein R is hydrogen;

R is methyl; and

R is hydrogen.

6. The compound according to claim 2 wherein R is methyl;

R is methyl; and

R is hydrogen.

7. Compounds according to claim 1 wherein Z is a carbon-carbon double bond;

each of X and Y is fluoro;

R is hydrogen; and

R R and R are as therein defined.

8. The compound according to claim 7 wherein R is hydrogen;

R is hydrogen; and

R is hydrogen.

9. The compound according to claim 7 wherein R is methyl;

R is hydrogen; and

R is hydrogen.

10. The compound according to claim 7 wherein R is hydrogen;

R is methyl; and

R is hydrogen.

11. The compound according to claim 7 wherein R is methyl;

R is methyl; and

R is hydrogen.

9 12. Compounds of the formula:

cu .c=c-R wherein 10 R is hydrogen, methyl, tetrahydropyranyl or a hydrocarbon carboxylic acyl group of less than 12 carbon atoms; R is hydrogen or methyl; 15

R is hydrogen, tetrahydropyranyl or a hydrocarbon carboxylic acyl group of less than 12 carbon atoms; and

R is hydrogen, methyl or chloro.

13. Compounds according to claim 12 wherein R is hydrogen; and

R R and R are as therein defined.

14. The compound according to claim 13 wherein 1 0 R is hydrogen; R is hydrogen; and R is hydrogen. 15. The compound according to claim 13 wherein R is methyl; R is hydrogen; and R is hydrogen. 16. The compound according to claim 13 wherein R is hydrogen; R is methyl; and R is hydrogen. 17. The compound according to claim 13 wherein R is methyl; R is methyl; and R is hydrogen.

References Cited Lehmann at 9.1.: Ber. Deut. Chem. Ges. 98, 14701475 (1956) (p. 1472 relied on).

LEWIS GOTTS, Primary Examiner. T. M. MESHBESHER, Assistant Examiner.

UNITED STATES PATENT OFFICE Patent No 3 ,385 ,871 May 28 1968 John A. Edwards, et a1.

It is certified that error appears in the above identified patent and that said Letters Patent are hereby corrected as shown below:

Column 7, line 61, "Z-methoxy" should read 3-methoxy Column 8, lines 32 and 37, "R", each occurrence, should read Y Signed and sealed this 2nd day of December 1969.

(SEAL) Attest:

Edward M. Fletcher, Jr.

Attesting Officer Commissioner of Patents WILLIAM E. SCHUYLER, JR. 

